A nurse is educating a client about the inheritance pattern of cystic fibrosis (CF). What information should the nurse provide regarding the likelihood of a child developing CF if both parents are carriers?
"If both parents are carriers, there is a 50% chance that their child will have CF."
"If both parents are carriers, their child is guaranteed to have CF."
"If both parents are carriers, their child will be a carrier but will not have CF."
"If both parents are carriers, their child will have a 25% chance of having CF."
The Correct Answer is D
A) Incorrect. If both parents are carriers, their child's risk of having CF is 25%, not 50%.
B) Incorrect. While the risk is increased, having two carrier parents does not guarantee that a child will have CF.
C) Incorrect. If both parents are carriers, their child can inherit two normal genes (no CF), one normal and one CF gene (carrier status), or two CF genes (CF).
D) Correct. When both parents are carriers, there is a 25% chance that their child will inherit two CF genes and have CF, a 50% chance of being a carrier, and a 25% chance of inheriting two normal genes (no CF).
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
A) Correct. Postural drainage and chest percussion help mobilize and remove thick, sticky mucus from the airways, which is crucial in managing CF.
B) Incorrect. While bronchodilators may be used, they are not the primary therapy for managing CF. Airway clearance techniques like postural drainage are more important.
C) Incorrect. Oxygen therapy should be administered as needed, but it is not required around the clock for all CF patients.
D) Incorrect. Deep breathing exercises should be encouraged regularly, not just during illness, to maintain airway clearance and lung function.
Correct Answer is B
Explanation
A) Incorrect. Genetic testing can confirm CF but is not typically the initial diagnostic test used in infants with symptoms suggestive of CF.
B) Correct. The sweat chloride test is often used as the initial diagnostic test to assess for CF in infants who exhibit symptoms.
C) Incorrect. Chest X-rays may be used to assess lung changes in individuals with CF but are not typically the initial diagnostic test in infants.
D) Incorrect. Pulmonary function tests are used to evaluate lung function but are not typically the initial diagnostic test for CF in infants.
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